Amphibole genesis via metasomatic reaction with clinopyroxene in mantle xenoliths from Victoria Land, Antarctica
Introduction
Mantle xenoliths from Mt. Melbourne and Mt. Overlord (Victoria Land, Antarctica) occur in scoria cones and in basanitic to tephritic lavas. Alkaline to tholeiitic magmatism in this area started in the early Eocene in relation to the Ross Sea Rift system, which is situated along the eastern border of the Transantarctic mountains Fitzgerald et al., 1987, Beccaluva et al., 1991a. The rift system is organized in two main branches: one inland, trending NNW–SSE up to Mt. Overlord, while the other, toward the sea, is directed NE–SW. Petrological features and thermobarometric evolution of the lithospheric mantle from Cape Washington to Mt. Overlord were discussed in Beccaluva et al. (1991b), and more recently by Perinelli and Armienti (2002). However, several peculiar petrographic and geochemical features related to the widespread presence of amphibole remain untreated. In particular, the occurrence (and the strict association in several xenoliths) of amphibole, clinopyroxene and glasses provides a unique opportunity for investigating amphibole formation in relation to metasomatism, eventually leading to the hydration of anhydrous mantle.
It is well-known that amphibole represents a key mineral in mantle paragenesis as it is one of the main hosts for alkalis. Its role is crucial in basalt petrogenesis even at high degrees of partial melting (Beccaluva et al., 1998), as well as in mantle glass genesis via decompression or in situ melting processes Chazot et al., 1996a, Yaxley and Kamenetsky, 1999, Yaxley et al., 1997.
Disseminated amphibole growing around clinopyroxene and/or spinel is commonly observed Francis, 1976, Fabriés et al., 1987, Vaselli et al., 1996, Gregoire et al., 1997, Dawson and Smith, 1988, Bodinier et al., 1990, Zanetti et al., 1996, Woodland et al., 1996, Moine et al., 2001, Ionov et al., 2002, though its genesis is often referred to previous, generally poorly defined, metasomatic event/s Zanetti et al., 1996, Witt-Eickschen et al., 1998. Zanetti et al. (1996) distinguish two kinds of disseminated amphiboles: one older, produced by a previous metasomatism, and one younger, occurring only in the proximity of amphibole veins, related to the infiltration into the wall-rock by the same liquid generating the veins. On the other hand, vein amphiboles are usually considered products of direct crystallization from basanite or alkali basalt magmas in the upper mantle Francis, 1976, O'Reilly, 1987, O'Reilly et al., 1991, Dawson and Smith, 1988, Ionov et al., 1997, Witt-Eickschen et al., 1998, Moine et al., 2001. The residual melt afterward infiltrates the peridotite matrix, creating new amphibole in the form of crystallization or reaction products.
Some inconsistency arises in those models where disseminated amphiboles are (i) older and separated from the magmatic event which created the vein amphibole, even if chemical composition may be quite comparable and, in any case, leaving the petrogenesis of disseminated amphibole unsolved; or (ii) younger and formed by differentiated melts, even if major element contents (especially mg#) are very similar, and melt propagating through fracturing precedes porous flow migration. Thus, notwithstanding the large amount of papers reported above, the chemical and temporal relationships between disseminated and vein amphibole is still a matter of considerable debate. Moreover, to the best of the authors' knowledge, glasses related to amphibole formation have not been reported. Most studies regarding amphibole genesis were, in fact, developed on alpine peridotite massifs Woodland et al., 1996, McPherson et al., 1996, Zanetti et al., 1996 where glass cannot be preserved, or else in mantle xenoliths where amphibole and glass were related to either decompressional (Laurora et al., 2001) or in situ melting Chazot et al., 1996a, Yaxley and Kamenetsky, 1999 of volatile-bearing phases; in both cases amphibole is consumed, and glass plus secondary phases are produced.
As it will be shown below, amphibole in lithospheric mantle from Antarctica is growing at the expense of clinopyroxene and is always associated with glass, thus offering a unique opportunity to study the genetic processes (and metasomatic agent/s) responsible for its formation. To this purpose a painstaking petrographic study was accompanied by a major and trace element microanalytical work mainly addressing clinopyroxene, amphibole (disseminated in the peridotite matrix and in the vein) and glass compositional variations. The effects of host basalt infiltration were also studied in order to isolate host basalt contamination from metasomatic processes. Finally, a comparison between petrological features of the inferred metasomatic agent/s, and the basalts of the Ross Sea Rift system is presented, setting metasomatism and magmatism within a unique framework.
Of particular interest is the paper of Gamble and Kyle (1987), who studied an amphibole-glass-bearing wehrlite from Foster Crater (Antarctica) with textural features identical to those observed in the Mt. Melbourne peridotites; their data and model for amphibole, glass and host magma relationships were, in our opinion, really outstanding for the time. Our investigations however include also lherzolites, thus extending the study to more “common” mantle parageneses. Moreover, the interpretation of Gamble and Kyle (1987) of glasses as simple differentiation products from magmas similar to the host basalts after amphibole crystallization does not agree with our study.
Samples were collected during the Italian Antarctic expedition in the late 1980s. Numbers refer to localities, while letters indicate different xenoliths. Amphibole-bearing peridotites occur mainly in one locality north of Mt. Melbourne and, subordinately, in another west of Mt. Overlord. The studied samples represent all the amphibole-bearing xenoliths found (see also Beccaluva et al., 1991b for further description).
Section snippets
Petrography
The Antarctic xenoliths consist of both anhydrous and hydrous (mainly amphibole-bearing) lherzolites. Protogranular is the most common primary texture on which several types of secondary pyrometamorphic (metasomatic) textures are superimposed Mercier and Nicolas, 1975, Pike and Schwartzam, 1977. Hydrous peridotites are characterized by disseminated amphiboles in the peridotite matrix, and in veins: the former are always associated with spinel (Fig. 1A,C) and clinopyroxene (Fig. 1B,D), sometimes
Analytical methods
Major element analyses of minerals and glasses were carried out on a Cameca SX100 electron microprobe at the Institute of Petrology, Vienna University, the operating conditions were 15 kV and 20 nA. In order to reduce alkali loss, glass analyses were performed using a defocused beam with a diameter of 5–10 μm at 15kV and 10nA. The error for all elements is below 5%, except for Na, which may be up to 10%. Natural and synthetic standards were used for calibration, and the PAP correction (Pouchou
Phase geochemistry
The following description will be mainly focussed on compositional variations of clinopyroxene, amphibole and glass, thus neglecting olivine and spinel, whose variations in relation to metasomatism have already been discussed by several authors (Bonadiman et al., 2001, and references therein). As is usually observed for anhydrous parageneses, secondary olivine tends to be higher in mg# [Mg/(Mg+FeT) at.%] and spinel higher in cr# [Cr/(Cr+Al) at.%] compared to their primary counterparts.
Metasomatic melt/s and relationships with the Ross Sea magmatic system
The reactions which eventually lead to amphibole formation are modelled by mass balance calculations, which also made it possible to highlight the chemical characteristics of the metasomatic agents. The mass balance model is based on major element composition of primary and secondary minerals, with the metasomatic melt as the unknown. Reaction coefficients, obtained assuming a least-squares residue always <1.0 (Table 4), were then used for trace element calculations combined with the reactive
Evolutionary model
The distinction between contamination by the host basalt during (or shortly before) the uprising and metasomatism, i.e. infiltration of magmas at mantle level, is not at all straightforward, particularly when the metasomatic melt has comparable geochemical features to the host basalt, and could hence be considered as part of a continuous process ultimately leading to magma formation. In order to present the evolutionary model starting from metasomatic enrichment through amphibole formation up
Disseminated and vein amphiboles
As reported in the Phase geochemistry section, disseminated and vein amphiboles have similar major and trace element compositions (Fig. 4), which is a peculiar feature of Antarctic amphiboles.
Most of the disseminated and vein amphiboles reported in literature, in fact, show remarkable differences both in major and trace element distribution between the two types Dawson and Smith, 1988, Ionov et al., 1997, Moine et al., 2001.
In amphibole-bearing peridotites, amph-D growing around and in reaction
Conclusions
The petrographic and geochemical features of composite amphibole-bearing xenoliths from Antarctica indicate that amphibole is formed by reaction between the metasomatic melt and primary anhydrous parageneses, mainly at the expense of clinopyroxene and spinel. Clinopyroxene is the mineral that records the widest compositional variation during this reaction, and was probably pre-LREE-enriched through diffusion processes. It increases its TiO2, Al2O3 and HREE contents when the melt comes into
Acknowledgments
The authors are indebted to S. O'Reilly, G. Yaxley and A. Woodland for their constructive reviews. Woodland in particular made a series of pertinent comments, which allowed us to better constrain the first draft of the reaction model.
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CO<inf>2</inf> storage in the Antarctica Sub-Continental Lithospheric Mantle as revealed by intra- and inter-granular fluids
2022, LithosCitation Excerpt :A similar model was proposed for Gobernador Gregores (Patagonia) mantle xenoliths by Scambelluri et al. (2009), who hypothesized that the FI were entrapped into minerals in strict association with the progressive degassing of alkali basalts during ascent, or, alternatively, by melting of peridotite-forming hydrous phases during xenoliths decompression and concomitant CO2-fluxing. As already modelled by Coltorti et al. (2004) and Perinelli et al. (1998), glasses in the studied NVL represent a melt phase that infiltrated the xenoliths shortly before their entrainment by the host basalt, generated as product of the reaction induced by the infiltration of alkaline metasomatic agents into the local SCLM. The concentration of volatiles trapped in FI is strongly dependant on the density of FI within each crystal and the entrapment P (Frezzotti et al., 2002), therefore a careful evaluation of the CO2 distribution within the studied samples must be made in order to filter the results for eventual dependencies on depth and/or degassing processes.